Abstract An 8-year-old girl was admitted for a simple closure of echocardiographically diagnosed Atrial Septal Defect (ASD). During the operation the right pulmonary veins orifices were not detected in the left atrium and attempt to localize them led to the discovery of three additional anomalies, namely Interrupted Inferior Vena Cava (IIVC), Scimitar syndrome, and systemic arterial supply of the lung. Postoperatively these finding were confirmed by CT angiography. This case report emphasizes the need for adequate preoperative diagnosis and presents a very rare constellation of four congenital anomalies that to the best of our knowledge is not reported before.</p
In this case report we describe the delayed diagnosis of a very rare congenital anomaly — isolated p...
Background: Anomalous pulmonary venous connection (APVC) is a rare, life threatening congenital hear...
Background: Anomalous pulmonary venous connection (APVC) is a rare, life threatening congenital hear...
Partial anomalous pulmonary vein connection (PAPVC) is a rare congenital abnormal cardiac defect inv...
An 11-year-old boy affected by pulmonary atresia with intact ventricular septum (AP-IVS) was listed ...
A case of an asymptomatic 4-year-old girl with hemodynamically significant type II atrial septal def...
Partial anomalous pulmonary venous connec-tion (PAPVC) is a condition in which some, but not all, pu...
A case of an asymptomatic 4-year-old girl with hemodynamically significant type II atrial septal def...
A case of an asymptomatic 4-year-old girl with hemodynamically significant type II atrial septal def...
Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital heart disease. Among prev...
A four-year-old girl presented with superior vena cava (SVC) type of sinus venosus defect, right upp...
Ttransesophageal echocardiography in an asymptomatic nine-month-old girl discerned features of an in...
A 7-month-old girl with failure to thrive, who, on clinical and diagnostic evaluation [echocardiogra...
Total drainage of systemic blood into the left atrium is an exceptional finding in the absence of se...
Over the years, different techniques have been introduced for the repair of sinus venosus atrial sep...
In this case report we describe the delayed diagnosis of a very rare congenital anomaly — isolated p...
Background: Anomalous pulmonary venous connection (APVC) is a rare, life threatening congenital hear...
Background: Anomalous pulmonary venous connection (APVC) is a rare, life threatening congenital hear...
Partial anomalous pulmonary vein connection (PAPVC) is a rare congenital abnormal cardiac defect inv...
An 11-year-old boy affected by pulmonary atresia with intact ventricular septum (AP-IVS) was listed ...
A case of an asymptomatic 4-year-old girl with hemodynamically significant type II atrial septal def...
Partial anomalous pulmonary venous connec-tion (PAPVC) is a condition in which some, but not all, pu...
A case of an asymptomatic 4-year-old girl with hemodynamically significant type II atrial septal def...
A case of an asymptomatic 4-year-old girl with hemodynamically significant type II atrial septal def...
Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital heart disease. Among prev...
A four-year-old girl presented with superior vena cava (SVC) type of sinus venosus defect, right upp...
Ttransesophageal echocardiography in an asymptomatic nine-month-old girl discerned features of an in...
A 7-month-old girl with failure to thrive, who, on clinical and diagnostic evaluation [echocardiogra...
Total drainage of systemic blood into the left atrium is an exceptional finding in the absence of se...
Over the years, different techniques have been introduced for the repair of sinus venosus atrial sep...
In this case report we describe the delayed diagnosis of a very rare congenital anomaly — isolated p...
Background: Anomalous pulmonary venous connection (APVC) is a rare, life threatening congenital hear...
Background: Anomalous pulmonary venous connection (APVC) is a rare, life threatening congenital hear...